Are n-BuLi/TMEDA-Mediated Arene Ortholithiations Directed? Substituent-Dependent Rates, Substituent-Independent Mechanisms | Journal of the American Chemical Society
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29 Si CPMAS NMR spectra of (a) carrier C, (b) C treated with BuLi, and... | Download Scientific Diagram
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Metalation of Pyridines with nBuLi−Li−Aminoalkoxide Mixed Aggregates: The Origin of Chemoselectivity | Journal of the American Chemical Society
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Lewis acid–catalyzed domino generation/[2,3]-sigmatropic rearrangement of ammonium ylides to access chiral azabicycles | Science Advances
R)‐BINOL‐6,6'‐bistriflone: Shortened Synthesis, Characterization, and Enantioselective Catalytic Applications - Mouhtady - 2021 - European Journal of Organic Chemistry - Wiley Online Library
n-Butyllithium/N,N,N',N'-Tetramethylethylenediamine-Mediated Ortholithiations of Aryl Oxazolines: Substrate-Dependent Mechanisms | Journal of the American Chemical Society
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364750-80-1|(2S,4R)-1-(tert-Butoxycarbonyl)-4-methylpyrrolidine-2-carboxylic acid| Ambeed
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NMR and DFT Studies with a Doubly Labelled 15N/6Li S‐Trifluoromethyl Sulfoximine Reveal Why a Directed ortho‐Lithiation Requires an Excess of n‐ BuLi - Hédouin - Angewandte Chemie International Edition - Wiley Online Library
Organic Syntheses Procedure
